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Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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    Articles By : Ruchika Sharma

    Cipla, Macleods HIV child treatments approved in South Africa

    Cipla, Macleods HIV child treatments approved in South Africa

    Ruchika Sharma27 Jun 2022 12:30 PM IST
    New Delhi: South Africa, which has the world's biggest number of people infected with HIV, has approved Cipla Ltd.'s quadrimune, a treatment for...
    Govt advisory panel to review trial data on Serum Institute qHPV vaccine against cervical cancer

    Govt advisory panel to review trial data on Serum Institute qHPV vaccine against cervical cancer

    Ruchika Sharma27 Jun 2022 11:29 AM IST
    New Delhi: The government advisory panel NTAGI is likely to review on June 28 trial data on India's first quadrivalent human papillomavirus (qHPV)...
    Bristol Myers Squibb bags USFDA nod for CAR T Cell Therapy Breyanzi

    Bristol Myers Squibb bags USFDA nod for CAR T Cell Therapy Breyanzi

    Ruchika Sharma26 Jun 2022 4:00 PM IST
    Breyanzi, a differentiated CAR T cell therapy, is made from a patient's own T cells, which are collected and genetically reengineered to become CAR T...
    Sinovac Biotech COVID vaccine CoronaVac conditionally registered in South Africa

    Sinovac Biotech COVID vaccine CoronaVac conditionally registered in South Africa

    Ruchika Sharma26 Jun 2022 2:30 PM IST
    China: Sinovac Biotech Ltd. has announced that the South African Health Products Regulatory Authority (SAHPRA) has granted conditional registration to...
    Novavax COVID vaccine Nuvaxovid recommended for expanded conditional marketing authorization in EU for adolescents

    Novavax COVID vaccine Nuvaxovid recommended for expanded conditional marketing authorization in EU for adolescents

    Ruchika Sharma26 Jun 2022 12:30 PM IST
    NVX-CoV2373 is a protein-based vaccine engineered from the genetic sequence of the first strain of SARS-CoV-2, the virus that causes COVID-19 disease.
    Valneva COVID vaccine gets marketing authorization in Europe

    Valneva COVID vaccine gets marketing authorization in Europe

    Ruchika Sharma26 Jun 2022 10:00 AM IST
    VLA2001 is the whole virus, inactivated, adjuvanted COVID-19 vaccine.
    Pfizer sets sights on elimination of blinding disease trachoma by 2030

    Pfizer sets sights on elimination of blinding disease trachoma by 2030

    Ruchika Sharma26 Jun 2022 9:00 AM IST
    The ITI had initially hoped to eliminate the disease by 2020, but is now setting its sights on 2030.
    Bristol Myers Squibb must face USD 6.4 billion lawsuit over delayed cancer drug

    Bristol Myers Squibb must face USD 6.4 billion lawsuit over delayed cancer drug

    Ruchika Sharma25 Jun 2022 3:30 PM IST
    The case arose from the company's agreement to pay Celgene shareholders holding "contingent value rights" an extra $9 per share in cash if it won U.S....
    Delhi HC Orders Arbitration in Medikabazaar Board Dispute, Tiwari Challenges Termination

    Delhi HC relief to Intas- Stops two pharma companies from violating trademark of LOOZ

    Ruchika Sharma25 Jun 2022 2:30 PM IST
    New Delhi: The Delhi High Court has permanently restrained two pharmaceutical manufacturers from using the trademark 'LOOZOUT' in their products,...
    BioNTech in conflict with regulator over new COVID vaccine nod: WAS newspaper

    BioNTech in conflict with regulator over new COVID vaccine nod: WAS newspaper

    Ruchika Sharma25 Jun 2022 1:30 PM IST
    The reason for this was that the approval "should go through the same regulatory process as ordinary flu vaccines", which would allow the new COVID-19...
    CDSCO panel recommends emergency use nod for SII Covovax for kids aged 7 to 11 years

    CDSCO panel recommends emergency use nod for SII Covovax for kids aged 7 to 11 years

    Ruchika Sharma25 Jun 2022 12:45 PM IST
    The recommendation has been sent to Drugs Controller General of India (DCGI) for final approval.
    USFDA concludes inspection at Dr Reddys Labs Srikakulam API facility

    Dr Reddys acquires injectable product portfolio from Eton Pharma for Rs 391 crore

    Ruchika Sharma25 Jun 2022 11:49 AM IST
    "The acquisition supports Dr. Reddy's efforts to accelerate and expand affordable medications for patients," the company stated.
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